Opportunity Description
Senior Site Specialist
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
The Role:
As a Senior Site Specialist, you will be responsible for completing country and/or regional clinical trial regulatory deliverables in line with study specifics, ensuring compliance with ICH-GCP, relevant regulations, and sound scientific principles. You will also contribute to process improvement initiatives, mentor junior staff as needed, and provide strategic input into submissions planning.
Key Responsibilities:
Deliver regulatory submissions in accordance with contractual timelines, budget, and quality standards.
Apply advanced knowledge of ICON SOPs/WIs, ICH-GCP, and local regulatory requirements.
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